A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3621726



Internal ID7008593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:124843049..124849474hg38UCSC Ensembl
Innerchr9:124843549..124848974hg38UCSC Ensembl
Outerchr9:124842049..124850474hg38UCSC Ensembl
chr9:127605328..127611753hg19UCSC Ensembl
Innerchr9:127605828..127611253hg19UCSC Ensembl
Outerchr9:127604328..127612753hg19UCSC Ensembl
Cytoband9q33.3
Allele length
AssemblyAllele length
hg386426
hg196426
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13618749, essv13618756, essv13618753, essv13618750, essv13618754, essv13618757, essv13618758, essv13618755, essv13618752, essv13618751
SamplesHG02840, HG02603, NA19651, NA19917, HG02819, HG02881, HG04152, HG02682, NA19438, NA19121
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3621726
Frequency
Sample Size2504
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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